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Cytal® Wound Matrix and MicroMatrix® Wound Study

Wounds Clinical Trial

Official title:
Use of Cytal® Wound Matrix and MicroMatrix® for the Management of Wounds

Clinical Trial Summary

This is an observational study to assess the safety and efficacy of MicroMatrix® alone or in combination with Cytal® Wound Matrix on primary measures of wound healing.

Clinical Trial Description

A single-site, prospective, observational clinical study of Cytal® Wound Matrix alone or in combination with MicroMatrix® for the management of wounds. Up to 100 patients with multiple wound types including but not limited to, venous ulcers, diabetic foot ulcers, trauma wounds, and external surgical wounds will be treated either with Cytal® Wound Matrix alone or with Cytal® Wound Matrix and MicroMatrix® for wounds exceeding 3mm in depth. Wound healing efficacy, effect of treatment on patient-reported quality of life, complete wound management, wound-related adverse event, and wound pathology will be measured. The protocol defined patient follow-up is 12 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03632954
Study type Observational
Source Integra LifeSciences Corporation
Contact
Status Terminated
Phase
Start date December 11, 2018
Completion date January 27, 2020
View Details
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